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[Cancer Research 65, 686-691, February 1, 2005]
© 2005 American Association for Cancer Research


Priority Reports

Hyaluronic Acid Induces Osteopontin via the Phosphatidylinositol 3-Kinase/Akt Pathway to Enhance the Motility of Human Glioma Cells

Mi-Suk Kim1,3, Myung-Jin Park2, Eui-Jung Moon1, So-Jeong Kim1, Chang-Hun Lee1, Heon Yoo1, Sang-Hoon Shin1, Eun-Sook Song3 and Seung-Hoon Lee1

1 Research Institute and Hospital, National Cancer Center, Goyang, Gyeonggi, Korea; 2 Laboratory of Cell Biology, Korea Institute of Radiological and Medical Sciences, and 3 Department of Life Science, Sookmyung Women's University, Seoul, Korea

Requests for reprints: Seung-Hoon Lee, National Cancer Center, 809 Madu-dong, Ilsan-gu, Goyang, Gyeonggi 411-764, Korea. Phone: 82-31-920-1660; Fax: 82-31-920-1520; E-mail: nslsh{at}ncc.re.kr.

Hyaluronic acid (HA) binds to cell-surface receptors such as CD44, and seems to be involved in cell adhesion, motility, and tumor progression in brain. To identify gene expression changes that are initiated by HA, we explored human cytokine arrays in U87MG glioma cells and identified osteopontin, a secreted matrix protein, as a transcriptional target of HA. Interestingly, expression of osteopontin was induced by HA in glioma cells lacking functional PTEN, a tumor suppressor gene (U87MG, U251MG, and U373MG), but not in wild-type (wt)-PTEN-harboring cells (LN18 and LN428). To confirm the role of PTEN, adenoviral (Ad)-wt-PTEN was used to induce ectopic expression of wt-PTEN in U87MG cells, leading to reduced HA-mediated osteopontin induction. Reciprocally, transfection with dominant-negative Akt repressed HA-induced osteopontin expression. Furthermore, HA promoted the motility of glioma cells, and down-regulation of induced osteopontin activity via a neutralizing anti-osteopontin antibody repressed HA-induced motility in vitro. Together, these results strongly suggest that induction of osteopontin expression by HA is dependent on activation of the phosphatidylinositol 3-kinase/Akt pathway. Furthermore, our data indicate that PTEN can effectively modulate the expression of osteopontin, and HA-induced osteopontin plays an important role in the motility response induced by HA in human glioma cells.

Key Words: hyaluronic acid • osteopontin • PTEN • motility • glioma




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2005 by the American Association for Cancer Research.